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15 results for “Mauremys”
Fig. 4 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)
Fig. 4. Linear regression of body weight (BW) on carapace length (CL) for Mauremys leprosa (N = 43).
Figure 3 in A new record of the freshwater turtle Mauremys rivulata (Valenciennes, 1833) in the Ofkos river, Cyprus: Conservation actions required
Figure 3. Turtle trap used for the research (upper right and lower left). Trap with two trapped individuals (upper left).
Fig. 3 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)
Fig. 3. Size structure of the population of Mauremys leprosa.
Fig. 2 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)
Fig. 2. Morphometrical variables of Mauremys leprosa (for abbreviations see table 3).
Figure 2 in A new record of the freshwater turtle Mauremys rivulata (Valenciennes, 1833) in the Ofkos river, Cyprus: Conservation actions required
Figure 2. Ponds where fresh water turtles were trapped.
Nest site selection and nesting behavior of Reeves’ turtle (Mauremys reevesii) in Qichun County, Hubei Province, China
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Data from: Density-dependent unidirectional hybridization between the Japanese pond turtle, Mauremys japonica and the exotic Reeves' pond turtle, Mauremys reevesii in Japan, inferred from molecular and morphological analyses
<p>Hybridisation between the indigenous Japanese pond turtle, <em>Mauremys japonica</em>, and the exotic Reeves' pond turtle, <em>Mauremys reevesii</em>, is widespread in Japan. In this study, we examined this hybridisation using an analysis of mtDNA and 11 microsatellite markers (MS) combined with morphometry. In a Bayesian clustering analysis of MS, the admixture of two clusters equivalent to the two species was detected in the Seto Inland Sea and Ise Bay regions. While mtDNA showed reciprocal hybridisation between the two species, their hybrids tended to possess the mtDNA of the rarer species at each locality. Contrary to preceding studies, F2/later generations outnumbered F1 generations. In addition, the admixture of two mtDNA lineages (Chinese and Korean) of <em>M. reevesii</em> was widely observed in all regions, together with the range expansion of the recently introduced Chinese lineage. A significant correlation was observed between plastron morph and assignment probability of MS, showing that plastron morphology reflects the degree of introgression by <em>M. reevesii</em> in <em>M. japonica</em>. This finding means that the reproductive interference of the dominant species on a rarer species is a major factor driving the hybridisation of the two Mauremys species. In addition, the range expansion of the Chinese lineage of M. reevesii appears to enhance the introgression by <em>M. reevesii</em> in <em>M. japonica</em>.</p>
Fig. 4 in Conservation genetics and phylogeography of the poorly known Middle Eastern terrapin Mauremys caspica (Testudines: Geoemydidae)
Fig. 4 Distribution of mitochondrial haplotypes of Mauremys caspica. Green symbols correspond to the western haplotype cluster; beige symbols, to the eastern cluster. The overlapping symbols (arrow) represent a syntopic occurrence of haplotypes of the two clusters. Numbers indicate individual haplotypes; numbers separated by slashes, syntopic occurrences of respective haplotypes. New haplotypes identified in the present study are numbers 11–14. Inset Parsimony network showing mutational relationships of haplotypes. Symbol size corresponds to haplotype frequency. Small black circles are missing node haplotypes. Unless otherwise indicated, lines connecting haplotypes represent one mutational step
Fig. 3 in Conservation genetics and phylogeography of the poorly known Middle Eastern terrapin Mauremys caspica (Testudines: Geoemydidae)
Fig. 3 Posterior distributions of population demographic parameters for Mauremys caspica using MSVAR. Each line corresponds to the sum of posterior distributions of the four runs obtained for each cluster; colour code as in Fig. 2. Top Posterior distribution of the estimated time (in years ago) for each bottleneck. Bottom Posterior distribution of ancestral (N1) and present (N0) effective population sizes
Data from: Density-dependent unidirectional hybridization between the Japanese pond turtle, Mauremys japonica and the exotic Reeves’ pond turtle, Mauremys reevesii in Japan, inferred from molecular and morphological analyses
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Figure 1 in A new record of the freshwater turtle Mauremys rivulata (Valenciennes, 1833) in the Ofkos river, Cyprus: Conservation actions required
Figure 1. The study area (green) and drainage network of the Ofkos and Serrahis rivers. Satellite image from Sentinel-2 cloudless - httpss2maps.eu by EOX IT Services GmbH_ Copernicus Sentinel data.
Fig. 1 in Conservation genetics and phylogeography of the poorly known Middle Eastern terrapin Mauremys caspica (Testudines: Geoemydidae)
Fig. 1 ΔK values for K ranging from 1 to 9, showing the modal values for the runs corrected for null alleles (solid line) and the naïve runs (dashed line) of STRUCTURE
Fig. 2 in Conservation genetics and phylogeography of the poorly known Middle Eastern terrapin Mauremys caspica (Testudines: Geoemydidae)
Fig. 2 Population structuring in Mauremys caspica for K 04 (top) from the STRUCTURE run with the highest probability value. Within each cluster, an individual terrapin corresponds to one column that reflects its inferred ancestry. Individuals with mixed ancestries (below a threshold of 80 % for cluster membership) are indicated by asterisks. Colours of sampling sites in the map (bottom) correspond to STRUC- TURE clusters; slices indicate presence of individuals with mixed ancestries of respective clusters. Mixed ancestries are also indicated by shared subsets of lines encircling symbols. Upper-case letters refer to clusters; LM to terrapins from the local market of Bahrain. When null alleles are coded as recessive, clusters A and B are lumped together and two individuals with mixed ancestry are referred to this more inclusive cluster (cf. Table S1)
Identification of candidate genes associated with temperature-dependent sex determination of Reeves' Turtle (Mauremys reevesii) by genome-wide transcriptome analysis
GEO Series GSE98234. Mauremys reevesii. 9 samples. Type: Expression profiling by high throughput sequencing.
Identification and characterization of miRNAs in temperature-dependent sex determination (TSD) of Chinese pond turtles (Mauremys reevesii)
GEO Series GSE92957. Mauremys reevesii. 3 samples. Type: Non-coding RNA profiling by high throughput sequencing.
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